Home / 510(k) Clearances / K770466

510(k) K770466

STOCKINGS, RVS TM by Parke-Davis Co. — Product Code EQL

K770466 is an FDA 510(k) premarket notification submitted by Parke-Davis Co. for the device "STOCKINGS, RVS TM". The FDA issued a decision of Substantially Equivalent on March 28, 1977. The device falls under product code EQL (Laryngostroboscope), a Class I device regulated under 21 CFR 874.4750. Parke-Davis Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 28, 1977
Date Received
March 10, 1977
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Laryngostroboscope
Device Class
Class I
Regulation Number
874.4750
Review Panel
EN
Submission Type

Other clearances by Parke-Davis Co.

  • K861725 — INTRACATH INTRAVENOUS CATHETER PLACEMENT UNIT (December 4, 1986)
  • K862119 — DESERET FLO-THRU INJECTATE TEMPERATURE SENSOR (August 29, 1986)
  • K855120 — ATI DISPOSABLE BIOLOGICAL TEST PACK (June 18, 1986)
  • K860570 — ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICE (March 31, 1986)
  • K860290 — VIAPIC CENTRAL LINE CATHETER (March 18, 1986)
  • K852192 — DISPOSABLE STEAM BIOLOGICAL TEST PACK (November 1, 1985)
  • K841967 — DESERET THERMODILUTION CARDIAC OUTPUT (August 19, 1985)
  • K851327 — DESERET ARTERIAL CATHETER (June 14, 1985)
  • K852078 — SPECTRUM(TENTATIVE) (June 7, 1985)
  • K844840 — DESERET INTRODUCER SET (May 16, 1985)

Other clearances for product code EQL

  • K984521 — RIWO DRIVE SYSTEM 2302 WITH GENERATOR, SMALL MOTOR HANDLES, 8563.111, 8563.351 (March 17, 1999)
  • K921184 — RLS 9100 RHINO-LARYNGEAL STROBOSCOPE (May 28, 1992)
  • K921285 — 9105 RIGID TELESCOPIC ENDOSCOPE (May 28, 1992)
  • K884933 — ENDOSTROBOSCOPE IV (February 15, 1989)
  • K842090 — RHINO-LARYNX STROBOSCOPE TYPE 4914 (July 18, 1984)
  • K822523 — LARYNGOSTROBOSCOPE (September 9, 1982)
  • K801866 — PENTAX LARYNGO-STROBOSCOPE MODEL LS-1A (September 16, 1980)

FDA data resources